Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb10 |
A |
T |
8: 124,691,762 (GRCm39) |
M401K |
possibly damaging |
Het |
Ablim3 |
T |
A |
18: 61,978,922 (GRCm39) |
H203L |
probably damaging |
Het |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Aox1 |
T |
G |
1: 58,393,588 (GRCm39) |
D1249E |
possibly damaging |
Het |
Astn2 |
T |
C |
4: 65,353,423 (GRCm39) |
I1116V |
possibly damaging |
Het |
Atad3a |
T |
C |
4: 155,831,807 (GRCm39) |
D489G |
probably damaging |
Het |
Caln1 |
G |
T |
5: 130,646,719 (GRCm39) |
G52C |
probably damaging |
Het |
Clcn7 |
A |
G |
17: 25,374,359 (GRCm39) |
T467A |
probably damaging |
Het |
Col17a1 |
A |
T |
19: 47,654,979 (GRCm39) |
I599N |
possibly damaging |
Het |
Cul2 |
T |
A |
18: 3,429,593 (GRCm39) |
H547Q |
probably damaging |
Het |
Cxcl14 |
T |
C |
13: 56,440,320 (GRCm39) |
T80A |
probably damaging |
Het |
Dscaml1 |
T |
A |
9: 45,581,401 (GRCm39) |
Y407N |
probably damaging |
Het |
Edc4 |
T |
A |
8: 106,611,748 (GRCm39) |
I108N |
probably damaging |
Het |
Exoc2 |
T |
C |
13: 31,124,720 (GRCm39) |
|
probably benign |
Het |
Gm1110 |
T |
G |
9: 26,807,916 (GRCm39) |
H290P |
probably benign |
Het |
Gm16223 |
T |
A |
5: 42,225,336 (GRCm39) |
W12R |
unknown |
Het |
Herc2 |
C |
A |
7: 55,878,317 (GRCm39) |
H4623Q |
probably damaging |
Het |
Igkv18-36 |
A |
T |
6: 69,969,589 (GRCm39) |
H68Q |
possibly damaging |
Het |
Kif7 |
T |
C |
7: 79,357,301 (GRCm39) |
E635G |
probably benign |
Het |
Or2t47 |
T |
C |
11: 58,442,388 (GRCm39) |
K226E |
probably benign |
Het |
Or4c109 |
A |
T |
2: 88,817,931 (GRCm39) |
I205N |
possibly damaging |
Het |
Or52z13 |
T |
A |
7: 103,246,574 (GRCm39) |
M17K |
possibly damaging |
Het |
Or9m1b |
A |
T |
2: 87,836,239 (GRCm39) |
N285K |
probably damaging |
Het |
Pam |
C |
A |
1: 97,792,054 (GRCm39) |
A456S |
probably benign |
Het |
Pgap3 |
T |
C |
11: 98,289,764 (GRCm39) |
T76A |
possibly damaging |
Het |
Pkd2 |
C |
A |
5: 104,637,215 (GRCm39) |
Y609* |
probably null |
Het |
Plcg2 |
A |
G |
8: 118,310,234 (GRCm39) |
D362G |
probably damaging |
Het |
Polr3h |
C |
A |
15: 81,801,595 (GRCm39) |
A94S |
probably benign |
Het |
Rhod |
T |
C |
19: 4,482,186 (GRCm39) |
D76G |
probably damaging |
Het |
Rims2 |
T |
C |
15: 39,320,129 (GRCm39) |
V670A |
probably damaging |
Het |
Rpap3 |
G |
A |
15: 97,579,620 (GRCm39) |
T464M |
possibly damaging |
Het |
Rufy1 |
T |
A |
11: 50,297,310 (GRCm39) |
I381L |
probably benign |
Het |
Slc1a4 |
T |
C |
11: 20,256,506 (GRCm39) |
T442A |
probably damaging |
Het |
Slc9b1 |
T |
C |
3: 135,100,670 (GRCm39) |
S472P |
probably damaging |
Het |
Tmtc3 |
T |
C |
10: 100,287,294 (GRCm39) |
T501A |
possibly damaging |
Het |
Tnpo3 |
C |
A |
6: 29,555,181 (GRCm39) |
D801Y |
probably damaging |
Het |
Ttc39b |
T |
C |
4: 83,179,193 (GRCm39) |
Y111C |
probably damaging |
Het |
Ubr4 |
A |
T |
4: 139,127,240 (GRCm39) |
R543* |
probably null |
Het |
Vps45 |
T |
G |
3: 95,960,401 (GRCm39) |
E80A |
probably benign |
Het |
Zfp677 |
T |
C |
17: 21,617,107 (GRCm39) |
Y55H |
probably damaging |
Het |
Zng1 |
A |
G |
19: 24,900,130 (GRCm39) |
V289A |
probably benign |
Het |
|
Other mutations in Vmn1r74 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01608:Vmn1r74
|
APN |
7 |
11,581,560 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01673:Vmn1r74
|
APN |
7 |
11,581,317 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03023:Vmn1r74
|
APN |
7 |
11,581,257 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0393:Vmn1r74
|
UTSW |
7 |
11,581,242 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1488:Vmn1r74
|
UTSW |
7 |
11,581,510 (GRCm39) |
missense |
probably benign |
0.02 |
R1707:Vmn1r74
|
UTSW |
7 |
11,581,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R1998:Vmn1r74
|
UTSW |
7 |
11,581,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1999:Vmn1r74
|
UTSW |
7 |
11,581,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R2139:Vmn1r74
|
UTSW |
7 |
11,581,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Vmn1r74
|
UTSW |
7 |
11,580,898 (GRCm39) |
missense |
probably damaging |
0.98 |
R4576:Vmn1r74
|
UTSW |
7 |
11,580,696 (GRCm39) |
splice site |
probably null |
|
R4619:Vmn1r74
|
UTSW |
7 |
11,581,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4619:Vmn1r74
|
UTSW |
7 |
11,581,398 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5371:Vmn1r74
|
UTSW |
7 |
11,580,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R5606:Vmn1r74
|
UTSW |
7 |
11,580,822 (GRCm39) |
missense |
probably benign |
0.01 |
R6464:Vmn1r74
|
UTSW |
7 |
11,581,131 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6901:Vmn1r74
|
UTSW |
7 |
11,581,368 (GRCm39) |
missense |
probably benign |
0.00 |
R6920:Vmn1r74
|
UTSW |
7 |
11,581,575 (GRCm39) |
missense |
probably benign |
0.01 |
R7223:Vmn1r74
|
UTSW |
7 |
11,580,894 (GRCm39) |
nonsense |
probably null |
|
R7231:Vmn1r74
|
UTSW |
7 |
11,580,888 (GRCm39) |
missense |
probably benign |
0.34 |
R7418:Vmn1r74
|
UTSW |
7 |
11,581,081 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8135:Vmn1r74
|
UTSW |
7 |
11,581,530 (GRCm39) |
missense |
probably benign |
0.36 |
R8692:Vmn1r74
|
UTSW |
7 |
11,580,972 (GRCm39) |
missense |
probably benign |
0.03 |
R8748:Vmn1r74
|
UTSW |
7 |
11,580,903 (GRCm39) |
missense |
probably benign |
0.10 |
R9004:Vmn1r74
|
UTSW |
7 |
11,580,840 (GRCm39) |
missense |
probably benign |
0.00 |
R9258:Vmn1r74
|
UTSW |
7 |
11,580,999 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9564:Vmn1r74
|
UTSW |
7 |
11,581,534 (GRCm39) |
missense |
probably damaging |
1.00 |
RF049:Vmn1r74
|
UTSW |
7 |
11,581,067 (GRCm39) |
frame shift |
probably null |
|
RF063:Vmn1r74
|
UTSW |
7 |
11,581,067 (GRCm39) |
frame shift |
probably null |
|
Z1176:Vmn1r74
|
UTSW |
7 |
11,580,936 (GRCm39) |
missense |
probably benign |
|
|